Julie Tibbets Email & Phone Number

Julie Tibbets chairs Goodwin’s Life Sciences Regulatory & Compliance practice and co-chairs Goodwin's Rare Disease Initiative. She focuses her practice on FDA-regulated product development, crisis resolution, product marketing and corporate communications as well as the intersection of each of those with corporate strategy and securities disclosure obligations. Her product areas of focus include biologics, drugs, medical devices, in vitro diagnostics, as well as digital therapeutics, tools and apps. Julie advises clients on product development strategy, interactions with the FDA, clinical trial conduct and documentation, crisis management, adverse event reporting, commercial strategy, product labeling and advertising and FDA inspections and enforcement. She also leads internal regulatory compliance investigations and due diligence reviews of FDA-regulated entities across a wide range of transactions from public offerings to M&A deals and private equity investments.

Listed skills include Fda, Medical Devices, Marketing Communications, Pharmaceutical Industry, and 11 others.